HuGE Literature Finder
Records 1-5
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The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).
Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
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Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.
Journal of clinical immunology 2012 Dec 32 (6): 1165-79. Kutukculer Necil, Gulez Nesrin, Karaca Neslihan E, Aksu Guzide, Berdeli Af |
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Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency.
Journal of investigational allergology & clinical immunology 2011 21 (5): 348-53. Tampella G, Baronio M, Vitali M, Soresina A, Badolato R, Giliani S, Plebani A, Lougaris |
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B-cell numbers in the blood of patients with non-HLA*B8 or non-HLA*B44 common variable immunodeficiency.
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology 2007 Feb 98 (2): 163-7. Johnston Douglas T, Schroeder Harry |
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Polymorphisms of human CD19 gene: possible association with susceptibility to systemic lupus erythematosus in Japanese.
Genes and immunity 2002 Oct 3 Suppl 1 (): S21-30. Kuroki K, Tsuchiya N, Tsao B P, Grossman J M, Fukazawa T, Hagiwara K, Kano H, Takazoe M, Iwata T, Hashimoto H, Tokunaga |
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- Page last updated:Sep 23, 2021
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